Identification and Characterization of Soluble Isoform of Fibroblast Growth Factor Receptor 3 in Human SaOS-2 Osteosarcoma Cells
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference21 articles.
1. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes
2. Fibroblast growth factor receptor 2 mutations in Beare–Stevenson cutis gyrata syndrome
3. Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans
4. Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3
5. Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
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3. Phenotypic and Signaling Consequences of a Novel Aberrantly Spliced Transcript FGF Receptor-3 in Hepatocellular Carcinoma;Cancer Research;2016-06-07
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